Variant report

Variant	nsv1035231
Chromosome Location	chr12:63537412-63582333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:368)
CpG islands
(count:856)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:63545234-63545470	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:63544074-63544342	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr12:63550104-63550132	GM12878	blood:	n/a	n/a
4	CBX3	chr12:63570065-63570332	K562	blood:	n/a	n/a
5	CEBPB	chr12:63569654-63569734	IMR90	lung:	n/a	chr12:63569707-63569718
6	CEBPB	chr12:63569649-63569765	A549	lung:	n/a	chr12:63569707-63569718
7	CEBPB	chr12:63577350-63577566	HepG2	liver:	n/a	chr12:63577475-63577486
8	CEBPB	chr12:63572887-63573147	A549	lung:	n/a	n/a
9	CEBPB	chr12:63572966-63573073	K562	blood:	n/a	n/a
10	CEBPB	chr12:63577407-63577618	A549	lung:	n/a	chr12:63577475-63577486
11	CEBPB	chr12:63572869-63573101	IMR90	lung:	n/a	n/a
12	CEBPB	chr12:63569647-63569844	HepG2	liver:	n/a	chr12:63569707-63569718
13	CEBPB	chr12:63573010-63573086	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:63554623-63554689	A549	lung:	n/a	n/a
15	CHD1	chr12:63544502-63544718	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr12:63544525-63544972	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr12:63543928-63544259	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr12:63543651-63545351	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr12:63545060-63545210	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr12:63545940-63546090	HCFaa	heart:	n/a	chr12:63546025-63546038
21	CTCF	chr12:63545960-63546110	HCM	heart:	n/a	chr12:63546025-63546038
22	CTCF	chr12:63545960-63546110	HCT-116	colon:	n/a	chr12:63546025-63546038
23	CTCF	chr12:63546000-63546150	HepG2	liver:	n/a	chr12:63546025-63546038
24	CTCF	chr12:63545821-63546243	GM12878	blood:	n/a	chr12:63546025-63546038
25	CTCF	chr12:63546000-63546150	HAc	cerebellar:	n/a	chr12:63546025-63546038
26	CTCF	chr12:63546200-63546350	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr12:63545680-63545830	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr12:63545940-63546090	RPTEC	kidney:	n/a	chr12:63546025-63546038
29	CTCF	chr12:63545700-63545746	GM19238	blood:	n/a	n/a
30	CTCF	chr12:63544480-63544630	AG04449	skin:	n/a	n/a
31	CTCF	chr12:63545980-63546130	HRPEpiC	eye:	n/a	chr12:63546025-63546038
32	CTCF	chr12:63545100-63545250	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr12:63545560-63545710	WI-38	lung:	n/a	n/a
34	CTCF	chr12:63546140-63546290	GM12870	blood:	n/a	n/a
35	CTCF	chr12:63545980-63546130	HUVEC	blood vessel:	n/a	chr12:63546025-63546038
36	CTCF	chr12:63545980-63546130	GM12864	blood:	n/a	chr12:63546025-63546038
37	CTCF	chr12:63545869-63546131	MCF-7	breast:	n/a	chr12:63546025-63546038
38	CTCF	chr12:63545694-63545832	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:63545940-63546090	GM12869	blood:	n/a	chr12:63546025-63546038
40	CTCF	chr12:63546320-63546470	GM12864	blood:	n/a	n/a
41	CTCF	chr12:63545866-63546157	ProgFib	skin:	n/a	chr12:63546025-63546038
42	CTCF	chr12:63545980-63546130	BJ	skin:	n/a	chr12:63546025-63546038
43	CTCF	chr12:63545881-63546146	LNCaP	prostate:	n/a	chr12:63546025-63546038
44	CTCF	chr12:63545900-63546050	HFF	foreskin:	n/a	chr12:63546025-63546038
45	CTCF	chr12:63545960-63546110	AG09309	skin:	n/a	chr12:63546025-63546038
46	CTCF	chr12:63545844-63546156	Fibrobl	skin:	n/a	chr12:63546025-63546038
47	CTCF	chr12:63545900-63546050	WI-38	lung:	n/a	chr12:63546025-63546038
48	CTCF	chr12:63545870-63546200	ECC-1	luminal epithelium:	n/a	chr12:63546025-63546038
49	CTCF	chr12:63545888-63546161	Hela-S3	cervix:	n/a	chr12:63546025-63546038
50	CTCF	chr12:63545640-63545790	GM12868	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63545956-63546006	HNPCEpiC	eye:	n/a
2	chr12:63544923-63544973	BE2_C	brain:	n/a
3	chr12:63545956-63546006	HNPCEpiC	eye:	n/a
4	chr12:63544923-63544973	BE2_C	brain:	n/a
5	chr12:63543831-63543881	HNPCEpiC	eye:	n/a
6	chr12:63547716-63547766	AG09309	skin:	n/a
7	chr12:63543292-63543342	AG04450	lung:	fetal
8	chr12:63544857-63544907	PrEC	prostate:	n/a
9	chr12:63545783-63545833	HL-60	blood:	n/a
10	chr12:63545288-63545338	ProgFib	skin:	n/a
11	chr12:63545783-63545833	GM19239	blood:	n/a
12	chr12:63544319-63544369	U87	brain:	n/a
13	chr12:63543292-63543342	HCT-116	colon:	n/a
14	chr12:63544923-63544973	AG10803	skin:	n/a
15	chr12:63545523-63545573	NT2-D1	testis:	n/a
16	chr12:63543292-63543342	AG09319	gingival:	n/a
17	chr12:63544430-63544480	BJ	skin:	n/a
18	chr12:63546263-63546313	ovcar-3	ovarian:	n/a
19	chr12:63545956-63546006	HCPEpiC	choroid plexus:	n/a
20	chr12:63543292-63543342	HCF	heart:	n/a
21	chr12:63545783-63545833	SK-N-MC	brain:	n/a
22	chr12:63546263-63546313	GM12878	blood:	n/a
23	chr12:63543292-63543342	IMR90	lung:	fetal
24	chr12:63545523-63545573	SKMC	muscle:	n/a
25	chr12:63544923-63544973	MCF-7	breast:	n/a
26	chr12:63544175-63544225	PANC-1	pancreas:	n/a
27	chr12:63540400-63540450	NHBE	bronchial:	n/a
28	chr12:63544857-63544907	HMEC	breast:	n/a
29	chr12:63544857-63544907	HEK293	kidney:	embryo
30	chr12:63546263-63546313	HEEpiC	esophagus:	n/a
31	chr12:63546263-63546313	AG04450	lung:	fetal
32	chr12:63545956-63546006	NT2-D1	testis:	n/a
33	chr12:63547716-63547766	A549	lung:	n/a
34	chr12:63543831-63543881	NHDF-neo	bronchial:	n/a
35	chr12:63544319-63544369	T-47D	breast:	n/a
36	chr12:63544319-63544369	IMR90	lung:	fetal
37	chr12:63545523-63545573	AG04450	lung:	fetal
38	chr12:63544319-63544369	NH-A	brain:	n/a
39	chr12:63544430-63544480	HMEC	breast:	n/a
40	chr12:63544923-63544973	HCF	heart:	n/a
41	chr12:63544923-63544973	T-47D	breast:	n/a
42	chr12:63544430-63544480	Caco-2	colon:	n/a
43	chr12:63540400-63540450	AoSMC	blood vessel:	n/a
44	chr12:63544319-63544369	BJ	skin:	n/a
45	chr12:63545956-63546006	AG10803	skin:	n/a
46	chr12:63544319-63544369	SAEC	small airway:	n/a
47	chr12:63544857-63544907	Hepatocyte	liver:	n/a
48	chr12:63546263-63546313	HCF	heart:	n/a
49	chr12:63544430-63544480	HRPEpiC	eye:	n/a
50	chr12:63545288-63545338	AG09319	gingival:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63545448..63546470-chr12:63670124..63671316,6	MCF-7	breast:
2	chr12:62996207..62999162-chr12:63547684..63549229,2	MCF-7	breast:
3	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
4	chr12:63545428..63546206-chr12:63674883..63675724,2	MCF-7	breast:
5	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
6	chr12:63545559..63546473-chr12:63669896..63671149,5	MCF-7	breast:
7	chr12:63535701..63537481-chr12:63551924..63553918,2	MCF-7	breast:
8	chr12:63535701..63537481-chr12:63551924..63553918,2	MCF-7	breast:
9	chr12:63545419..63546376-chr12:64195555..64196413,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM5-5	chr12:63563605-63563746	l_664_chr12:63563604-63657550_brain
2	lnc-TMEM5-5	chr12:63563762-63563912	l_664_chr12:63563604-63657550_brain
3	lnc-TMEM5-5	chr12:63580624-63580735	l_664_chr12:63563604-63657550_brain
4	lnc-MON2-3	chr12:63547640-63547786	ENSG00000257973.1
5	lnc-MON2-3	chr12:63546261-63546418	ENSG00000257973.1
6	lnc-MON2-3	chr12:63544845-63544872	ENSG00000257973.1

No data

Variant related genes	Relation type
AVPR1A	TF binding region
AVPR1A	CpG island
ENSG00000221949	chromatin interactions
ENSG00000199179	chromatin interactions
ENSG00000257354	chromatin interactions

Extended variants
information (count: 715 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11174808	chr12:63537412-63537413	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150602242	chr12:63537449-63537450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372201548	chr12:63537465-63537466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192931772	chr12:63537467-63537468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73327829	chr12:63537530-63537531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546609144	chr12:63537567-63537568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112553967	chr12:63537598-63537599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544018499	chr12:63537705-63537706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371249505	chr12:63537708-63537709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529353630	chr12:63537732-63537733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557486283	chr12:63537736-63537737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577860283	chr12:63537746-63537747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545050691	chr12:63537776-63537777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184776582	chr12:63537790-63537791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374491878	chr12:63537805-63537806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56408178	chr12:63537890-63537891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187923758	chr12:63537912-63537913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192995890	chr12:63537939-63537940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558136457	chr12:63537961-63537962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571933531	chr12:63537990-63537991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183770229	chr12:63537996-63537997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560173592	chr12:63538033-63538034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188300257	chr12:63538045-63538046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542792091	chr12:63538067-63538068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34269762	chr12:63538078-63538079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10047514	chr12:63538122-63538123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs576193609	chr12:63538129-63538130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181807722	chr12:63538172-63538173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565003176	chr12:63538177-63538178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35115440	chr12:63538178-63538179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527586928	chr12:63538189-63538190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540193852	chr12:63538229-63538230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115703722	chr12:63538239-63538240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529341160	chr12:63538254-63538255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549091588	chr12:63538270-63538271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11829406	chr12:63538273-63538274	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs10877967	chr12:63538275-63538276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs531394393	chr12:63538288-63538289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79701458	chr12:63538294-63538295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200282238	chr12:63538323-63538324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149808818	chr12:63538373-63538374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369217927	chr12:63538431-63538432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11829452	chr12:63538449-63538450	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547414617	chr12:63538454-63538455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10747983	chr12:63538458-63538459	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs75882052	chr12:63538470-63538471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556261163	chr12:63538482-63538483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576108791	chr12:63538521-63538522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184985187	chr12:63538560-63538561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10784339	chr12:63538646-63538647	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63531000-63538400	Weak transcription	Liver	Liver
2	chr12:63537400-63537800	Enhancers	Adipose Nuclei	Adipose
3	chr12:63537400-63538000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:63537800-63540400	Weak transcription	Adipose Nuclei	Adipose
5	chr12:63538000-63539800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:63538400-63540400	Strong transcription	Liver	Liver
7	chr12:63539800-63540200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr12:63540200-63540600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:63540400-63540600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
10	chr12:63540400-63541000	Genic enhancers	Liver	Liver
11	chr12:63540400-63541200	Active TSS	Psoas Muscle	Psoas
12	chr12:63540400-63543200	Active TSS	Adipose Nuclei	Adipose
13	chr12:63540600-63541000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr12:63541000-63541200	Weak transcription	Liver	Liver
15	chr12:63541000-63542600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:63541200-63541400	Flanking Active TSS	Liver	Liver
17	chr12:63541200-63541400	Flanking Active TSS	Psoas Muscle	Psoas
18	chr12:63541400-63543800	Active TSS	Liver	Liver
19	chr12:63541800-63542200	Weak transcription	Psoas Muscle	Psoas
20	chr12:63542000-63543200	Active TSS	Fetal Muscle Leg	muscle
21	chr12:63542200-63542400	Bivalent/Poised TSS	Fetal Brain Female	brain
22	chr12:63542200-63543400	Active TSS	Fetal Stomach	stomach
23	chr12:63542600-63543800	Bivalent/Poised TSS	Right Ventricle	heart
24	chr12:63542600-63545200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:63542800-63545000	Bivalent Enhancer	Fetal Brain Male	brain
26	chr12:63543000-63543200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
27	chr12:63543000-63543800	Bivalent/Poised TSS	Fetal Brain Female	brain
28	chr12:63543200-63543600	Active TSS	Fetal Muscle Trunk	muscle
29	chr12:63543200-63543600	Active TSS	Psoas Muscle	Psoas
30	chr12:63543200-63543800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
31	chr12:63543200-63543800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
32	chr12:63543200-63543800	Bivalent/Poised TSS	Left Ventricle	heart
33	chr12:63543200-63543800	Active TSS	Right Atrium	heart
34	chr12:63543200-63544000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
35	chr12:63543200-63546400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr12:63543400-63543600	Enhancers	Pancreas	Pancrea
37	chr12:63543400-63543800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:63543400-63543800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr12:63543400-63543800	Bivalent/Poised TSS	Fetal Stomach	stomach
40	chr12:63543400-63543800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
41	chr12:63543600-63543800	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:63543600-63543800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
44	chr12:63543600-63543800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
45	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
46	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
47	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:63543600-63543800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
49	chr12:63543600-63543800	Bivalent Enhancer	Fetal Intestine Small	intestine
50	chr12:63543600-63543800	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle

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